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Altered glutamate receptor function in the cerebellum of the Ppt1(−/−) mouse, a murine model of infantile neuronal ceroid lipofuscinosis

The neuronal ceroid lipofuscinoses (NCLs) are a family of devastating pediatric neurodegenerative disorders and currently represent the most common form of pediatric-onset neurodegeneration. Infantile NCL (INCL), the most aggressive of these disorders, is caused by mutations in the CLN1 gene that en...

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Autors principals: Finn, Rozzy, Kovács, Attila D., Pearce, David A.
Format: Artigo
Idioma:Inglês
Publicat: 2011
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3237775/
https://ncbi.nlm.nih.gov/pubmed/21971706
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jnr.22763
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